Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers

Triblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-...

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Main Authors: Chung Sol Kim, Seung Soo Park, Sung Dong Kim, Su Jin Kwon, Jun Won Baek, Bun Yeoul Lee
Format: Article
Language:English
Published: MDPI AG 2017-10-01
Series:Polymers
Subjects:
Online Access:https://www.mdpi.com/2073-4360/9/10/481
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spelling doaj-7e226a8a3c0747fea92760864a3ae43d2020-11-25T00:53:14ZengMDPI AGPolymers2073-43602017-10-0191048110.3390/polym9100481polym9100481Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block CopolymersChung Sol Kim0Seung Soo Park1Sung Dong Kim2Su Jin Kwon3Jun Won Baek4Bun Yeoul Lee5Department of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaTriblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-block-PS. We herein report a one-pot strategy for attaching PS chains to both ends of PO chains to construct PS-block-PO-block-PS directly from olefin and styrene monomers. Dialkylzinc compound containing styrene moieties ((CH2=CHC6H4CH2CH2)2Zn) was prepared, from which poly(ethylene-co-propylene) chains were grown via “coordinative chain transfer polymerization” using the pyridylaminohafnium catalyst to afford di-end functional PO chains functionalized with styrene and Zn moieties. Subsequently, PS chains were attached at both ends of the PO chains by introduction of styrene monomers in addition to the anionic initiator Me3SiCH2Li·(pmdeta) (pmdeta = pentamethyldiethylenetriamine). We found that the fraction of the extracted PS homopolymer was low (~20%) and that molecular weights were evidently increased after the styrene polymerization (ΔMn = 27–54 kDa). Transmission electron microscopy showed spherical and wormlike PS domains measuring several tens of nm segregated within the PO matrix. Optimal tensile properties were observed for the sample containing a propylene mole fraction of 0.25 and a styrene content of 33%. Finally, in the cyclic tensile test, the prepared copolymers exhibited thermoplastic elastomeric properties with no breakage up over 10 cycles, which is comparable to the behavior of commercial-grade SEBS.https://www.mdpi.com/2073-4360/9/10/481coordinative chain transfer polymerizationdi-end-functional polyolefinblock copolymerthermoplastic elastomer
collection DOAJ
language English
format Article
sources DOAJ
author Chung Sol Kim
Seung Soo Park
Sung Dong Kim
Su Jin Kwon
Jun Won Baek
Bun Yeoul Lee
spellingShingle Chung Sol Kim
Seung Soo Park
Sung Dong Kim
Su Jin Kwon
Jun Won Baek
Bun Yeoul Lee
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
Polymers
coordinative chain transfer polymerization
di-end-functional polyolefin
block copolymer
thermoplastic elastomer
author_facet Chung Sol Kim
Seung Soo Park
Sung Dong Kim
Su Jin Kwon
Jun Won Baek
Bun Yeoul Lee
author_sort Chung Sol Kim
title Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
title_short Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
title_full Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
title_fullStr Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
title_full_unstemmed Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
title_sort polystyrene chain growth from di-end-functional polyolefins for polystyrene-polyolefin-polystyrene block copolymers
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2017-10-01
description Triblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-block-PS. We herein report a one-pot strategy for attaching PS chains to both ends of PO chains to construct PS-block-PO-block-PS directly from olefin and styrene monomers. Dialkylzinc compound containing styrene moieties ((CH2=CHC6H4CH2CH2)2Zn) was prepared, from which poly(ethylene-co-propylene) chains were grown via “coordinative chain transfer polymerization” using the pyridylaminohafnium catalyst to afford di-end functional PO chains functionalized with styrene and Zn moieties. Subsequently, PS chains were attached at both ends of the PO chains by introduction of styrene monomers in addition to the anionic initiator Me3SiCH2Li·(pmdeta) (pmdeta = pentamethyldiethylenetriamine). We found that the fraction of the extracted PS homopolymer was low (~20%) and that molecular weights were evidently increased after the styrene polymerization (ΔMn = 27–54 kDa). Transmission electron microscopy showed spherical and wormlike PS domains measuring several tens of nm segregated within the PO matrix. Optimal tensile properties were observed for the sample containing a propylene mole fraction of 0.25 and a styrene content of 33%. Finally, in the cyclic tensile test, the prepared copolymers exhibited thermoplastic elastomeric properties with no breakage up over 10 cycles, which is comparable to the behavior of commercial-grade SEBS.
topic coordinative chain transfer polymerization
di-end-functional polyolefin
block copolymer
thermoplastic elastomer
url https://www.mdpi.com/2073-4360/9/10/481
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